Canonical Allele Identifier: CA3134472290

Gene: OSMR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38933376C= , CM000667.2:g.38933376C=	GRCh38
NC_000005.9:g.38933478C= , CM000667.1:g.38933478C=	GRCh37
NC_000005.8:g.38969235C=	NCBI36
NG_016236.1:g.92519C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003999.3:c.2872C= MANE Select	NP_003990.1:p.Pro958=
ENST00000274276.8:c.2872C= MANE Select	ENSP00000274276.3:p.Pro958=
NM_001323505.1:c.2872C=	NP_001310434.1:p.Pro958=
NM_001323505.2:c.2872C=	NP_001310434.1:p.Pro958=
NM_001323506.1:c.2875C=	NP_001310435.1:p.Pro959=
NM_001323506.2:c.2875C=	NP_001310435.1:p.Pro959=
NM_003999.2:c.2872C=	NP_003990.1:p.Pro958=
ENST00000274276.7:c.2872C=	ENSP00000274276.3:p.Pro958=
ENST00000508882.1:c.74+841C=
ENST00000509237.5:c.155+841C=
XM_005248384.1:c.2875C=	XP_005248441.1:p.Pro959=
XM_005248385.1:c.2875C=	XP_005248442.1:p.Pro959=
XM_011514161.1:c.2370+841C=	XP_011512463.1:n.2370+841C=
XM_011514161.2:c.2370+841C=	XP_011512463.1:n.2370+841C=
XM_017010019.1:c.2367+841C=	XP_016865508.1:n.2367+841C=
XR_925661.1:n.2759+841C=